Evidence map›Paper›PMID 38217649›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2024

Ribosome Profiling Methods Adapted to the Study of RNA-Dependent Translation Regulation in Staphylococcus aureus.

Maximilian P Kohl, Béatrice Chane-Woon-Ming, Roberto Bahena-Ceron, Jose Jaramillo-Ponce, Laura Antoine, Lucas Herrgott, Pascale Romby, Stefano Marzi

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Article in Methods in molecular biology (Clifton, N.J.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
6.0field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 4 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Maximilian P Kohl *Architecture et Réactivité de l'ARN, CNRS 9002, Université de Strasbourg, Strasbourg, France.
Béatrice Chane-Woon-Ming *Architecture et Réactivité de l'ARN, CNRS 9002, Université de Strasbourg, Strasbourg, France.
Roberto Bahena-Ceron *Architecture et Réactivité de l'ARN, CNRS 9002, Université de Strasbourg, Strasbourg, France.
Jose Jaramillo-PonceArchitecture et Réactivité de l'ARN, CNRS 9002, Université de Strasbourg, Strasbourg, France.
Laura AntoineArchitecture et Réactivité de l'ARN, CNRS 9002, Université de Strasbourg, Strasbourg, France.
Lucas HerrgottArchitecture et Réactivité de l'ARN, CNRS 9002, Université de Strasbourg, Strasbourg, France.
Pascale RombyArchitecture et Réactivité de l'ARN, CNRS 9002, Université de Strasbourg, Strasbourg, France.
Stefano MarziArchitecture et Réactivité de l'ARN, CNRS 9002, Université de Strasbourg, Strasbourg, France. S.Marzi@ibmc-cnrs.unistra.fr.
Centre National de la Recherche Scientifique · FRUniversité de Strasbourg · FRArchitecture et Réactivité de l'arN · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Noncoding RNAs, including regulatory RNAs (sRNAs), are instrumental in regulating gene expression in pathogenic bacteria, allowing them to adapt to various stresses encountered in their host environments. Staphylococcus aureus is a well-studied model for RNA-mediated regulation of virulence and pathogenicity, with sRNAs playing significant roles in shaping S. aureus interactions with human and animal hosts. By modulating the translation and/or stability of target mRNAs, sRNAs regulate the synthesis of virulence factors and regulatory proteins required for pathogenesis. Moreover, perturbation of the levels of RNA modifications in two other classes of noncoding RNAs, rRNAs, and tRNAs, has been proposed to contribute to stress adaptation. However, the study of how these various factors affect translation regulation has often been restricted to specific genes, using in vivo reporters and/or in vitro translation systems. Genome-wide sequencing approaches offer novel perspectives for studying RNA-dependent regulation. In particular, ribosome profiling methods provide a powerful resource for characterizing the overall landscape of translational regulation, contributing to a better understanding of S. aureus physiopathology. Here, we describe protocols that we have adapted to perform ribosome profiling in S. aureus.

Indexed as

Ribosome ProfilingStaphylococcus aureusAnimalsGene Expression RegulationGene Expression Regulation, BacterialHumansRNA, MessengerRNA, RibosomalRNA, MessengerRNA, RibosomalRibo-RETRibo-seqRibosome profilingStaphylococcus aureusStart codonsTranslation initiationTranslation regulation

Identifiers

PMID38217649
OpenAlexW4390843515

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.